Canonical Allele Identifier: CA299442760
Gene: LINC00907 HGNC NCBI

Linked Data

dbSNP Id: rs16976171

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.42479656G>T , CM000680.2:g.42479656G>T GRCh38
NC_000018.9:g.40059621G>T , CM000680.1:g.40059621G>T GRCh37
NC_000018.8:g.38313619G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046174.2:n.872+24667G>T
NR_046454.1:n.652+24667G>T
NR_046455.1:n.489+24667G>T